54
B. Schmidt
92. Srihari P, Kumaraswamy B, Rao GM, Yadav JS (2010) First stereoselective total synthesis of
(–)-stagonolide A. Tetrahedron: Asymmetry 21:106
93. Prabhakar P, Rajaram S, Reddy DK, Shekar V, Venkateswarlu Y (2010) Total synthesis of the
phytotoxic stagonolides A and B. Tetrahedron: Asymmetry 21:216
94. Mohapatra DK, Somaiah R, Rao MM, Caijo FD, Mauduit M, Yadav JS (2010) Catalytic
activity studies of aminocarbonyl group containing Hoveyda-Grubbs-type complexes for the
syntheses of herbarumin I and stagonolide A. Synlett 1223
95. Srihari P, Maheswara Rao G, Srinivasa Rao R, Yadav JS (2010) A stereoselective aldol
approach for the total synthesis of herbarumin I and stagonolide A. Synthesis 2407
96. Radha Krishna P, Ramana DV (2012) Titanium(IV)-promoted regioselective nucleophilic
ring-opening reaction of chiral epoxyallyl alcohols with acids as a tool for ready access to
chiral 1,2,3-triol monoesters: application to stereoselective total synthesis of macrolides. J
Org Chem 77:674
97. Srihari P, Kumaraswamy B, Yadav JS (2009) A carbohydrate approach for the synthesis of
tetrahydropyran containing C16-C29 fragment of sorangicin A. Tetrahedron 65:6304
98. Vadhadiya PM, Puranik VG, Ramana CV (2012) The total synthesis and structural revision
of stagonolide D. J Org Chem 77:2169
99. Angulo-Pachoón CA, Díaz-Oltra S, Murga J, Carda M, Marco JA (2010) Stereoselective
synthesis and structural correction of the naturally occurring lactone stagonolide G. Org Lett
12:5752
100. Giri AG, Mondal MA, Puranik VG, Ramana CV (2010) Effect of the allylic substituents on
ring closing metathesis: the total synthesis of stagonolide B and 4-epi-stagonolide B. Org
Biomol Chem 8:398
101. Srihari P, Kumaraswamy B, Somaiah R, Yadav JS (2010) The stereoselective total synthesis
of (+)-stagonolide B. Synthesis 1039
102. Jana N, Mahapatra T, Nanda S (2009) Chemo-enzymatic asymmetric total synthesis of
stagonolide C. Tetrahedron Asymmetry 20:2622
103. Wu J-Z, Wang Z, Qiao C (2012) Synthesis of stagonolide C from Mulzer epoxide. Tetrahedron
Lett 53:1153
104. Yadav JS, Mallikarjuna Reddy N, Venkateswar Rao N, Rahman MA, Prasad AR (2012)
Stereoselective total synthesis of stagonolide C. Helv Chim Acta 95:227
105. Venkatesham A, Nagaiah K (2012) Stereoselective total synthesis of stagonolide C. Tetrahedron: Asymmetry 23:1186
106. Shelke AM, Rawat V, Suryavanshi G, Sudalai A (2012) Asymmetric synthesis of (+)stagonolide C and (−)-aspinolide A via organocatalysis. Tetrahedron: Asymmetry 23:1534
107. Show K, Kumar P (2016) Synthesis of ophiocerins A, B and C, botryolide E, decarestrictine
O, stagonolide C and 9-epi-stagonolide C employing chiral hexane-1,2,3,5-tetraol derivatives
as building blocks. Eur J Org Chem 4696
108. Mahapatra T, Das T, Nanda S (2011) Asymmetric synthesis of stagonolide D and stagonolide
G. Bull Chem Soc Jpn 84:511
109. Kumar AS, Kumar JN, Kanth BS, Shinde DB, Das B (2018) Stereoselective total synthesis
of proposed structure of stagonolide D. Org Chem Curr Res 7:1000186
110. Sravanth Kumar A, Praneeth K, Srihari P, Yadav JS (2017) First stereoselective total synthesis
and reconfirmation of absolute structure of nonenolide (−)-stagonolide D. Tetrahedron Lett
58:509
111. Sabitha G, Padmaja P, Reddy PN, Jadav SS, Yadav JS (2010) Stereoselective total synthesis
of stagonolide E. Tetrahedron Lett 51:6166
112. Das T, Nanda S (2012) Chemoenzymatic total synthesis of stagonolide E. Tetrahedron Lett
53:256
113. Chatterjee S, Ghadigaonkar S, Sur P, Sharma A, Chattopadhyay S (2014) A chemoenzymatic synthesis of hept-6-ene-2,5-diol stereomers: application to asymmetric synthesis of
decarestrictine L, pyrenophorol, and stagonolide E. J Org Chem 79:8067
114. Rajaram S, Ramulu U, Aravind S, Suresh Babu K (2015) Stereoselective total synthesis of
stagonolide E. Helv Chim Acta 98:650
B. Schmidt
92. Srihari P, Kumaraswamy B, Rao GM, Yadav JS (2010) First stereoselective total synthesis of
(–)-stagonolide A. Tetrahedron: Asymmetry 21:106
93. Prabhakar P, Rajaram S, Reddy DK, Shekar V, Venkateswarlu Y (2010) Total synthesis of the
phytotoxic stagonolides A and B. Tetrahedron: Asymmetry 21:216
94. Mohapatra DK, Somaiah R, Rao MM, Caijo FD, Mauduit M, Yadav JS (2010) Catalytic
activity studies of aminocarbonyl group containing Hoveyda-Grubbs-type complexes for the
syntheses of herbarumin I and stagonolide A. Synlett 1223
95. Srihari P, Maheswara Rao G, Srinivasa Rao R, Yadav JS (2010) A stereoselective aldol
approach for the total synthesis of herbarumin I and stagonolide A. Synthesis 2407
96. Radha Krishna P, Ramana DV (2012) Titanium(IV)-promoted regioselective nucleophilic
ring-opening reaction of chiral epoxyallyl alcohols with acids as a tool for ready access to
chiral 1,2,3-triol monoesters: application to stereoselective total synthesis of macrolides. J
Org Chem 77:674
97. Srihari P, Kumaraswamy B, Yadav JS (2009) A carbohydrate approach for the synthesis of
tetrahydropyran containing C16-C29 fragment of sorangicin A. Tetrahedron 65:6304
98. Vadhadiya PM, Puranik VG, Ramana CV (2012) The total synthesis and structural revision
of stagonolide D. J Org Chem 77:2169
99. Angulo-Pachoón CA, Díaz-Oltra S, Murga J, Carda M, Marco JA (2010) Stereoselective
synthesis and structural correction of the naturally occurring lactone stagonolide G. Org Lett
12:5752
100. Giri AG, Mondal MA, Puranik VG, Ramana CV (2010) Effect of the allylic substituents on
ring closing metathesis: the total synthesis of stagonolide B and 4-epi-stagonolide B. Org
Biomol Chem 8:398
101. Srihari P, Kumaraswamy B, Somaiah R, Yadav JS (2010) The stereoselective total synthesis
of (+)-stagonolide B. Synthesis 1039
102. Jana N, Mahapatra T, Nanda S (2009) Chemo-enzymatic asymmetric total synthesis of
stagonolide C. Tetrahedron Asymmetry 20:2622
103. Wu J-Z, Wang Z, Qiao C (2012) Synthesis of stagonolide C from Mulzer epoxide. Tetrahedron
Lett 53:1153
104. Yadav JS, Mallikarjuna Reddy N, Venkateswar Rao N, Rahman MA, Prasad AR (2012)
Stereoselective total synthesis of stagonolide C. Helv Chim Acta 95:227
105. Venkatesham A, Nagaiah K (2012) Stereoselective total synthesis of stagonolide C. Tetrahedron: Asymmetry 23:1186
106. Shelke AM, Rawat V, Suryavanshi G, Sudalai A (2012) Asymmetric synthesis of (+)stagonolide C and (−)-aspinolide A via organocatalysis. Tetrahedron: Asymmetry 23:1534
107. Show K, Kumar P (2016) Synthesis of ophiocerins A, B and C, botryolide E, decarestrictine
O, stagonolide C and 9-epi-stagonolide C employing chiral hexane-1,2,3,5-tetraol derivatives
as building blocks. Eur J Org Chem 4696
108. Mahapatra T, Das T, Nanda S (2011) Asymmetric synthesis of stagonolide D and stagonolide
G. Bull Chem Soc Jpn 84:511
109. Kumar AS, Kumar JN, Kanth BS, Shinde DB, Das B (2018) Stereoselective total synthesis
of proposed structure of stagonolide D. Org Chem Curr Res 7:1000186
110. Sravanth Kumar A, Praneeth K, Srihari P, Yadav JS (2017) First stereoselective total synthesis
and reconfirmation of absolute structure of nonenolide (−)-stagonolide D. Tetrahedron Lett
58:509
111. Sabitha G, Padmaja P, Reddy PN, Jadav SS, Yadav JS (2010) Stereoselective total synthesis
of stagonolide E. Tetrahedron Lett 51:6166
112. Das T, Nanda S (2012) Chemoenzymatic total synthesis of stagonolide E. Tetrahedron Lett
53:256
113. Chatterjee S, Ghadigaonkar S, Sur P, Sharma A, Chattopadhyay S (2014) A chemoenzymatic synthesis of hept-6-ene-2,5-diol stereomers: application to asymmetric synthesis of
decarestrictine L, pyrenophorol, and stagonolide E. J Org Chem 79:8067
114. Rajaram S, Ramulu U, Aravind S, Suresh Babu K (2015) Stereoselective total synthesis of
stagonolide E. Helv Chim Acta 98:650