Facile Deprotection of 1,3‐Oxathiolanes to Carbonyl Compounds with O‐Iodoxy Benzoic Acid (IBX) in the Presence of β‐Cyclodextrin in WaterFootnote
IICT Communication No. 060424.

M. Somi Reddy Organic Chemistry Division I, Indian Institute of Chemical Technology, Hyderabad, India

M. Narender Organic Chemistry Division I, Indian Institute of Chemical Technology, Hyderabad, India

A. Mahesh Organic Chemistry Division I, Indian Institute of Chemical Technology, Hyderabad, India

Y. V. D. Nageswar Organic Chemistry Division I, Indian Institute of Chemical Technology, Hyderabad, India

K. Rama Rao Organic Chemistry Division I, Indian Institute of Chemical Technology, Hyderabad, IndiaCorrespondence[email protected]

Abstract

1,3‐Oxathiolanes are smoothly deprotected to carbonyl compounds by IBX at room temperature with β‐cyclodextrin as a catalyst and water as solvent.

IICT Communication No. 060424.

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Acknowledgment

M. S. R., M. N. and A. M. thank to CSIR, New Delhi, India, for financial assistance.

Notes

IICT Communication No. 060424.

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Facile Deprotection of 1,3‐Oxathiolanes to Carbonyl Compounds with O‐Iodoxy Benzoic Acid (IBX) in the Presence of β‐Cyclodextrin in WaterFootnote
IICT Communication No. 060424.

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Facile Deprotection of 1,3‐Oxathiolanes to Carbonyl Compounds with O‐Iodoxy Benzoic Acid (IBX) in the Presence of β‐Cyclodextrin in WaterFootnoteIICT Communication No. 060424.

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Facile Deprotection of 1,3‐Oxathiolanes to Carbonyl Compounds with O‐Iodoxy Benzoic Acid (IBX) in the Presence of β‐Cyclodextrin in WaterFootnote
IICT Communication No. 060424.